Abstract

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder resulting in cognitive decline or dementia, the number of patients with AD is continuously increasing. Although a lot of great progress has been made in research and development of AD therapeutics, there is no fundamental cure for this disease yet. This study demonstrated the memory-improving effects of Cuban policosanol (PCO) in 5xFAD mice, which is an animal model of AD. Following 4-months of treatment with PCO in 5xFAD mice, we found that the number of amyloid plaques decreased in the brain compared to the vehicle-treated 5xFAD mice. Long-term PCO treatment in 5xFAD mice resulted in the reduction of gliosis and abnormal inflammatory cytokines level (interleukin [IL]-1β, IL-6, and tumor necrosis factor [TNF]-α) in the cortex and hippocampus. Levels of lipid peroxide (4-hydroxynonenal [4-HNE]) and superoxide dismutase (SOD1 and SOD2) levels were also recoverd in the brains of PCO-treated 5xFAD mice. Notably, PCO administration reduced memory deficits in the passive avoidance test, as well as synaptic loss (PSD-95, synaptophysin) in 5xFAD mice. Collectively, we identified the potential effects of PCO as a useful supplement to delay or prevent AD progression by inhibiting the formation of Aβ plaques in the brain.

Highlights

  • Alzheimer’s disease (AD) is a progressive neurodegenerative disease associated with cognitive decline

  • After the treatment of 2 months-old 5xFAD mice with PCO for 4 months, we examined the protective effect of PCO on memory deficits (Figure 1A)

  • Our results demonstrated that the PCO treatment attenuated astrogliosis attenuated astrogliosis in the 5xFAD mice

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Summary

Introduction

Alzheimer’s disease (AD) is a progressive neurodegenerative disease associated with cognitive decline. AD has a neuropathological hallmark consisting of extracellular amyloid plaque deposition composed of amyloid beta (Aβ) peptide and intracellular neurofibrillary tangles (NFT) containing hyperphosphorylated tau [2,3,4]. Amyloid plaques and NFT are mainly deposited in the brain, such as the hippocampus, entorhinal cortex, and basal forebrain, which influence learning, memory, and emotional behavior [5]. These neuropathologies result in damage and destruction of the synapses that mediate memory and cognition [6]. Research on the treatment of AD is continuously progressing, currently no clear preventive or therapeutic drugs exist

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